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Expression of Cyclin Kinase Inhibitor p21/WAF1 Protein in Pituitary Adenomas: Correlations with Endocrine Activity, but not Cell Proliferation.

Authors :
Hiyama, H.
Kubo, O.
Kawamata, T.
Ishizaki, R.
Hori, T.
Source :
Acta Neurochirurgica; May2002, Vol. 144 Issue 5, p481-488, 8p
Publication Year :
2002

Abstract

Summary. p21/WAF1 blocks cell cycle progression through inhibition of cyclin/cyclin-dependent kinases (cdks) complexes and, simultaneously, has been associated with cell cycle exit and the process of differentiation. In this series, the expression of p21/WAF1 was assessed immunohistochemically in 47 cases of pituitary adenomas in relation to endocrine activity and cell proliferation. To evaluate cell proliferation, a monoclonal antibody, MIB-1, against Ki-67 antigen was used in all of the available cases. The study revealed positive p21/WAF1 staining in 24 cases of 26 functioning parenchymas, whereas 14 cases of 21 non-functioning parenchymas stained negative. The MIB-1 index ranged from less than 1% to 5.1% (mean: less than 1.7%) in functioning adenomas, and from less than 1% to 3.6% (mean: less than 1.6%) in non-functioning adenomas. Regardless of endocrine activity, p21/WAF1 positivity did not correlate with the MIB-1 index. Double staining techniques revealed the co-expression of p21/WAF1/GH or p21/WAF1/PRL in functioning adenomas. In 22 cases of p21/WAF1-positive functioning adenomas, p21/WAF1 immunoreactivity was seen in the cytoplasma as well as nuclei. These results indicate that in pituitary adenomas, p21/WAF1 expression is associated with endocrine activity, but not with cell proliferation. Taken together with recent findings demonstrating that cytoplasmic p21/WAF1 acts as an inhibitor of apoptosis, it is possible that pituitary adenomas expressing cytoplasmic p21/WAF1 have resistance against DNA-damaging agents such as ionizing radiation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00016268
Volume :
144
Issue :
5
Database :
Complementary Index
Journal :
Acta Neurochirurgica
Publication Type :
Academic Journal
Accession number :
15395481
Full Text :
https://doi.org/10.1007/s007010200069